Canonical Allele Identifier: CA2579234171

Gene: RAD21 UTP23

Linked Data

• gnomAD v4: 8-116847768-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.116847771_116847772del , CM000670.2:g.116847771_116847772del	GRCh38
NC_000008.10:g.117860010_117860011del , CM000670.1:g.117860010_117860011del	GRCh37
NC_000008.9:g.117929191_117929192del	NCBI36
NG_032862.1:g.32097_32098del , LRG_772:g.32097_32098del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517485.6:c.1705-79_1705-78del (RAD21)	ENSP00000427923.2:n.1705-79_1705-78del
ENST00000517749.2:c.1705-79_1705-78del (RAD21)	ENSP00000430273.2:n.1705-79_1705-78del
ENST00000519837.6:c.1705-79_1705-78del (RAD21)	ENSP00000430524.2:n.1705-79_1705-78del
ENST00000520992.6:c.1705-79_1705-78del (RAD21)	ENSP00000429342.2:n.1705-79_1705-78del
ENST00000522699.2:c.1705-79_1705-78del (RAD21)	ENSP00000428158.2:n.1705-79_1705-78del
ENST00000523986.6:n.4674-79_4674-78del (RAD21)
ENST00000685972.1:n.5008-79_5008-78del (RAD21)
ENST00000687122.1:n.4533-79_4533-78del (RAD21)
ENST00000687358.1:c.1705-79_1705-78del (RAD21)	ENSP00000509687.1:n.1705-79_1705-78del
ENST00000687902.1:c.*80-79_*80-78del (RAD21)	ENSP00000510729.1:n.*80-79_*80-78del
ENST00000689124.1:n.1919-79_1919-78del (RAD21)
ENST00000689154.1:n.1518_1519del (RAD21)
ENST00000690166.1:n.6495_6496del (RAD21)
ENST00000297338.7:c.1705-79_1705-78del (RAD21) MANE Select	ENSP00000297338.2:n.1705-79_1705-78del
ENST00000297338.6:c.1705-79_1705-78del (RAD21)	ENSP00000297338.2:n.1705-79_1705-78del
ENST00000517749.1:c.19-79_19-78del (RAD21)	ENSP00000430273.1:n.19-79_19-78del
ENST00000517820.1:c.189-1117_189-1116del (UTP23)	ENSP00000427767.1:n.189-1117_189-1116del
ENST00000518055.1:c.340-79_340-78del (RAD21)	ENSP00000428003.1:n.340-79_340-78del
ENST00000520733.5:c.46-1117_46-1116del (UTP23)	ENSP00000429384.1:n.46-1117_46-1116del
ENST00000521703.5:c.*93-1117_*93-1116del (UTP23)	ENSP00000428455.1:n.*93-1117_*93-1116del
ENST00000523986.5:c.217-79_217-78del (RAD21)	ENSP00000428513.1:n.217-79_217-78del
ENST00000524128.1:c.*93-1117_*93-1116del (UTP23)	ENSP00000430309.1:n.*93-1117_*93-1116del
NM_006265.2:c.1705-79_1705-78del , LRG_772t1:c.1705-79_1705-78del (RAD21)	NP_006256.1:n.1705-79_1705-78del
XR_928356.1:n.663-1117_663-1116del (UTP23)
NM_006265.3:c.1705-79_1705-78del (RAD21) MANE Select	NP_006256.1:n.1705-79_1705-78del